1. Clinical and Virologic Effectiveness of Remdesivir Treatment for Severe Coronavirus Disease 2019 (COVID-19) in Korea: a Nationwide Multicenter Retrospective Cohort Study
- Author
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Seongman Bae, Eun Jung Lee, Ji-Yeon Kim, Sohyun Bae, Seung-Ji Kang, Kyong Ran Peck, Pyoeng Gyun Choe, Jae-Hoon Ko, Yoonseon Park, Heun Choi, Sung-Han Kim, Shinhyea Cheon, Ji Hyeon Baek, Seong Eun Kim, Joong Sik Eom, Yujin Sohn, Hyun-Ha Chang, Eun Young Heo, Yu Min Kang, Jung Wan Park, Baek-Nam Kim, Hye Jin Shi, Jung Yeon Heo, Sang Hyun Ra, Eun Jeong Joo, Bo young Lee, Jin-Won Chung, and Da Young Kim
- Subjects
Male ,medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Remdesivir ,Virologic ,Real-Time Polymerase Chain Reaction ,Antiviral Agents ,Clinical ,03 medical and health sciences ,0302 clinical medicine ,Pharmacotherapy ,Internal medicine ,Clinical endpoint ,Humans ,Medicine ,030212 general & internal medicine ,Symptom onset ,Aged ,Retrospective Studies ,Aged, 80 and over ,Cycle threshold ,Severe ,Alanine ,SARS-CoV-2 ,business.industry ,COVID-19 ,Retrospective cohort study ,General Medicine ,Infectious Diseases, Microbiology & Parasitology ,Middle Aged ,Viral Load ,Respiration, Artificial ,Adenosine Monophosphate ,COVID-19 Drug Treatment ,Baseline characteristics ,Original Article ,Female ,business ,Viral load - Abstract
Background Remdesivir is widely used for the treatment of coronavirus disease 2019 (COVID-19), but controversies regarding its efficacy still remain. Methods A retrospective cohort study was conducted to evaluate the effect of remdesivir on clinical and virologic outcomes of severe COVID-19 patients from June to July 2020. Primary clinical endpoints included clinical recovery, additional mechanical ventilator (MV) support, and duration of oxygen or MV support. Viral load reduction by hospital day (HD) 15 was evaluated by calculating changes in cycle threshold (Ct) values. Results A total of 86 severe COVID-19 patients were evaluated including 48 remdesivir-treated patients. Baseline characteristics were not significantly different between the two groups. Remdesivir was administered an average of 7.42 days from symptom onset. The proportions of clinical recovery of the remdesivir and supportive care group at HD 14 (56.3% and 39.5%) and HD 28 (87.5% and 78.9%) were not statistically different. The proportion of patients requiring MV support by HD 28 was significantly lower in the remdesivir group than in the supportive care group (22.9% vs. 44.7%, P = 0.032), and MV duration was significantly shorter in the remdesivir group (average, 1.97 vs. 5.37 days; P = 0.017). Analysis of upper respiratory tract specimens demonstrated that increases of Ct value from HD 1–5 to 11–15 were significantly greater in the remdesivir group than the supportive care group (average, 10.19 vs. 5.36; P = 0.007), and the slope of the Ct value increase was also significantly steeper in the remdesivir group (average, 5.10 vs. 2.68; P = 0.007). Conclusion The remdesivir group showed clinical and virologic benefit in terms of MV requirement and viral load reduction, supporting remdesivir treatment for severe COVID-19., Graphical Abstract
- Published
- 2021